{"id":37406,"date":"2024-01-26T08:22:18","date_gmt":"2024-01-26T13:22:18","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=37406"},"modified":"2024-03-08T04:38:48","modified_gmt":"2024-03-08T09:38:48","slug":"research-what-we-study-med12","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/research-what-we-study-med12\/","title":{"rendered":"MED12"},"content":{"rendered":"<p><span class=\"TextRun SCXW119509041 BCX0\" lang=\"EN\" xml:lang=\"EN\" data-contrast=\"auto\"><span class=\"NormalTextRun SCXW119509041 BCX0\">The information for this summary of <\/span><\/span><strong><span class=\"TextRun MacChromeBold SCXW119509041 BCX0\" lang=\"EN\" xml:lang=\"EN\" data-contrast=\"auto\"><span class=\"NormalTextRun SCXW119509041 BCX0\"><span class=\"notranslate\">MED12<\/span>-related syndrome<\/span><\/span><\/strong><span class=\"TextRun SCXW119509041 BCX0\" lang=\"EN\" xml:lang=\"EN\" data-contrast=\"auto\"><span class=\"NormalTextRun SCXW119509041 BCX0\"> comes from research publications. This is not meant to take the place of medical advice.<\/span><\/span><span class=\"EOP SCXW119509041 BCX0\" data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/med12\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full MED12 Gene Guide<\/strong><\/a><\/p>\n<p><span style=\"font-weight: 400;\">The online Gene Guide includes more information about <span class=\"notranslate\">MED12<\/span> such as the chance of having another child with this condition, behavior and development concerns linked to <span class=\"notranslate\">MED12<\/span>-related syndrome or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/span><\/p>\n<p><strong><span class=\"notranslate\">MED12<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>Hardikar syndrome<\/strong><span style=\"font-weight: 400;\">, <\/span><strong>Lujan syndrome<\/strong><span style=\"font-weight: 400;\">, <\/span><strong>X-linked Ohdo syndrome<\/strong><span style=\"font-weight: 400;\">, <\/span><strong>FG syndrome type 1<\/strong><span style=\"font-weight: 400;\">, <\/span><strong>Opitz-Kaveggia syndrome<\/strong><span style=\"font-weight: 400;\">, and <\/span><strong>nonspecific intellectual disability<\/strong><span style=\"font-weight: 400;\">. For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">MED12<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of MED12-related syndrome comes from research publications. This is not meant to take the place of medical advice.\u00a0 Click here for our full MED12 Gene Guide The online Gene Guide includes more information about MED12 such as the chance of having another child with this condition, behavior and development concerns [&hellip;]<\/p>\n","protected":false},"author":28,"featured_media":0,"parent":29,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-gene-card.php","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"acf":[],"_links":{"self":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/37406"}],"collection":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/users\/28"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=37406"}],"version-history":[{"count":11,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/37406\/revisions"}],"predecessor-version":[{"id":43234,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/37406\/revisions\/43234"}],"up":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/29"}],"wp:attachment":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/media?parent=37406"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}